Team:University College London/Protocols/Nanodrop

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<noinclude>{{:Team:University_College_London/templates/head|coverpicture=week4}}
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== Nanodrop ==
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== Nanodrop ==</noinclude>
Software ND-1000
Software ND-1000
Model:
Model:
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1.Initialise the spectrophotometer by pipetting 1 µ of clean water onto lower optic surface, lowering the lever arm and selecting ‘initialise’ in the ND-1000 software
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'''Step 1:''' Initialise the spectrophotometer by pipetting 1 µ of clean water onto lower optic surface, lowering the lever arm and selecting ‘initialise’ in the ND-1000 software
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2.Wipe and add elution buffer as negative control. Click blank in ND-1000 software
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'''Step 2:''' Wipe and add elution buffer as negative control. Click blank in ND-1000 software
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3.Wipe and add 1 µl sample
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'''Step 3:''' Wipe and add 1 µl sample
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4.On the software set lambda to 260nm
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'''Step 4:''' On the software set lambda to 260nm
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5.Lower the lever arm and click measure in ND-1000 software
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'''Step 5:''' Lower the lever arm and click measure in ND-1000 software
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6.Take readings for concentration and purity
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'''Step 6:''' Take readings for concentration and purity
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7.Once measurement complete, wipe surface
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'''Step 7:''' Once measurement complete, wipe surface
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<noinclude>{{:Team:University_College_London/templates/foot}}</noinclude>

Latest revision as of 17:28, 2 August 2012

Nanodrop

Software ND-1000 Model:

Step 1: Initialise the spectrophotometer by pipetting 1 µ of clean water onto lower optic surface, lowering the lever arm and selecting ‘initialise’ in the ND-1000 software

Step 2: Wipe and add elution buffer as negative control. Click blank in ND-1000 software

Step 3: Wipe and add 1 µl sample

Step 4: On the software set lambda to 260nm

Step 5: Lower the lever arm and click measure in ND-1000 software

Step 6: Take readings for concentration and purity

Step 7: Once measurement complete, wipe surface